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. 2009 Aug 14;85(2):264–272. doi: 10.1016/j.ajhg.2009.07.004

Table 4.

Association in the Replication Cohort

SNP Chromosome Position (bp – B36) Gene Alleles (A1/A2) SLIC Risk Allele A1 CEPH Frequency Typed Strand p Quant Effect Size p Case-Cont Frequency of A1 Cases Frequency of A1 controls Odds Ratio (95% CI)
rs12927866 80,209,823 CMIP T/C C 0.47 + 0.1623 −0.08 0.0955 0.39 0.30 1.5 (0.9-2.3)
rs4265801 80,222,553 CMIP T/G T 0.43 + 0.0182 −0.15 0.0214 0.43 0.56 1.6 (1.1-2.5)
rs16955705 80,230,851 CMIP C/A A 0.50 + 0.0238 −0.14 0.0257 0.48 0.36 1.6 (1.1-2.5)
rs16973771 83,018,079 ATP2C2 C/T T 0.48 + 0.0079 −0.14 0.0135 0.32 0.45 1.7 (1.1-2.7)
rs2875891 83,021,410 ATP2C2 T/C C 0.44 + 0.0668 −0.06 0.0802 0.29 0.37 1.5 (1.0-2.3)
rs8045507 83,022,078 ATP2C2 A/G G 0.48 + 0.0058 −0.15 0.0110 0.31 0.44 1.8 (1.1-2.7)

SNP alleles are given with the minor allele first. Putative risk alleles in the replication cohort are marked with an asterisk. p Quant shows the p value for the quantitative analysis. p < 0.05 are highlighted in bold. The odds ratio indicates the ratio of case/control odds for each additional copy of the putative risk allele. The 95% confidence intervals for the odds ratios of all significantly associated SNPs exceeded 1.0. The effect size is the estimated effect of each risk allele on the nonword-repetition score (in SD).